Reorganization of 3D genome architecture provides insights into pathogenesis of early fatty liver disease in laying hens

Abstract Background Fatty liver disease causes huge economic losses in the poultry industry due to its high occurrence and lethality rate. Three-dimensional (3D) chromatin architecture takes part in disease processing by regulating transcriptional reprogramming. The study is carried out to investiga...

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Main Authors: Yanli Liu, Zhuqing Zheng, Chaohui Wang, Yumeng Wang, Xi Sun, Zhouzheng Ren, Xin Yang, Xiaojun Yang
Format: Article
Language:English
Published: BMC 2024-03-01
Series:Journal of Animal Science and Biotechnology
Subjects:
Online Access:https://doi.org/10.1186/s40104-024-01001-y
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author Yanli Liu
Zhuqing Zheng
Chaohui Wang
Yumeng Wang
Xi Sun
Zhouzheng Ren
Xin Yang
Xiaojun Yang
author_facet Yanli Liu
Zhuqing Zheng
Chaohui Wang
Yumeng Wang
Xi Sun
Zhouzheng Ren
Xin Yang
Xiaojun Yang
author_sort Yanli Liu
collection DOAJ
description Abstract Background Fatty liver disease causes huge economic losses in the poultry industry due to its high occurrence and lethality rate. Three-dimensional (3D) chromatin architecture takes part in disease processing by regulating transcriptional reprogramming. The study is carried out to investigate the alterations of hepatic 3D genome and H3K27ac profiling in early fatty liver (FLS) and reveal their effect on hepatic transcriptional reprogramming in laying hens. Results Results show that FLS model is constructed with obvious phenotypes including hepatic visible lipid deposition as well as higher total triglyceride and cholesterol in serum. A/B compartment switching, topologically associating domain (TAD) and chromatin loop changes are identified by high-throughput/resolution chromosome conformation capture (HiC) technology. Targeted genes of these alternations in hepatic 3D genome organization significantly enrich pathways related to lipid metabolism and hepatic damage. H3K27ac differential peaks and differential expression genes (DEGs) identified through RNA-seq analysis are also enriched in these pathways. Notably, certain DEGs are found to correspond with changes in 3D chromatin structure and H3K27ac binding in their promoters. DNA motif analysis reveals that candidate transcription factors are implicated in regulating transcriptional reprogramming. Furthermore, disturbed folate metabolism is observed, as evidenced by lower folate levels and altered enzyme expression. Conclusion Our findings establish a link between transcriptional reprogramming changes and 3D chromatin structure variations during early FLS formation, which provides candidate transcription factors and folate as targets for FLS prevention or treatment.
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spelling doaj.art-6d04ce502b264b3d9340bbe64eb2e3552024-03-10T12:18:51ZengBMCJournal of Animal Science and Biotechnology2049-18912024-03-0115111510.1186/s40104-024-01001-yReorganization of 3D genome architecture provides insights into pathogenesis of early fatty liver disease in laying hensYanli Liu0Zhuqing Zheng1Chaohui Wang2Yumeng Wang3Xi Sun4Zhouzheng Ren5Xin Yang6Xiaojun Yang7College of Animal Science and Technology, Northwest A&F UniversityInstitute of Agricultural Biotechnology, Jingchu University of TechnologyCollege of Animal Science and Technology, Northwest A&F UniversityCollege of Animal Science and Technology, Northwest A&F UniversityCollege of Animal Science and Technology, Northwest A&F UniversityCollege of Animal Science and Technology, Northwest A&F UniversityCollege of Animal Science and Technology, Northwest A&F UniversityCollege of Animal Science and Technology, Northwest A&F UniversityAbstract Background Fatty liver disease causes huge economic losses in the poultry industry due to its high occurrence and lethality rate. Three-dimensional (3D) chromatin architecture takes part in disease processing by regulating transcriptional reprogramming. The study is carried out to investigate the alterations of hepatic 3D genome and H3K27ac profiling in early fatty liver (FLS) and reveal their effect on hepatic transcriptional reprogramming in laying hens. Results Results show that FLS model is constructed with obvious phenotypes including hepatic visible lipid deposition as well as higher total triglyceride and cholesterol in serum. A/B compartment switching, topologically associating domain (TAD) and chromatin loop changes are identified by high-throughput/resolution chromosome conformation capture (HiC) technology. Targeted genes of these alternations in hepatic 3D genome organization significantly enrich pathways related to lipid metabolism and hepatic damage. H3K27ac differential peaks and differential expression genes (DEGs) identified through RNA-seq analysis are also enriched in these pathways. Notably, certain DEGs are found to correspond with changes in 3D chromatin structure and H3K27ac binding in their promoters. DNA motif analysis reveals that candidate transcription factors are implicated in regulating transcriptional reprogramming. Furthermore, disturbed folate metabolism is observed, as evidenced by lower folate levels and altered enzyme expression. Conclusion Our findings establish a link between transcriptional reprogramming changes and 3D chromatin structure variations during early FLS formation, which provides candidate transcription factors and folate as targets for FLS prevention or treatment.https://doi.org/10.1186/s40104-024-01001-y3D chromatin architectureFatty liver diseaseFolateH3K27ac profilingTranscription reprogramming
spellingShingle Yanli Liu
Zhuqing Zheng
Chaohui Wang
Yumeng Wang
Xi Sun
Zhouzheng Ren
Xin Yang
Xiaojun Yang
Reorganization of 3D genome architecture provides insights into pathogenesis of early fatty liver disease in laying hens
Journal of Animal Science and Biotechnology
3D chromatin architecture
Fatty liver disease
Folate
H3K27ac profiling
Transcription reprogramming
title Reorganization of 3D genome architecture provides insights into pathogenesis of early fatty liver disease in laying hens
title_full Reorganization of 3D genome architecture provides insights into pathogenesis of early fatty liver disease in laying hens
title_fullStr Reorganization of 3D genome architecture provides insights into pathogenesis of early fatty liver disease in laying hens
title_full_unstemmed Reorganization of 3D genome architecture provides insights into pathogenesis of early fatty liver disease in laying hens
title_short Reorganization of 3D genome architecture provides insights into pathogenesis of early fatty liver disease in laying hens
title_sort reorganization of 3d genome architecture provides insights into pathogenesis of early fatty liver disease in laying hens
topic 3D chromatin architecture
Fatty liver disease
Folate
H3K27ac profiling
Transcription reprogramming
url https://doi.org/10.1186/s40104-024-01001-y
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